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Kinesin spindle protein (KSP) inhibitors. Part 6: Design and synthesis of 3,5-diaryl-4,5-dihydropyrazole amides as potent inhibitors of the mitotic kinesin KSP

Authors :
Paul J. Coleman
John D. Schreier
Christopher D. Cox
Mark E. Fraley
Robert M. Garbaccio
Carolyn A. Buser
Eileen S. Walsh
Kelly Hamilton
Robert B. Lobell
Keith Rickert
Weikang Tao
Ronald E. Diehl
Vicki J. South
Joseph P. Davide
Nancy E. Kohl
Youwei Yan
Lawrence Kuo
Thomayant Prueksaritanont
Chunze Li
Elizabeth A. Mahan
Carmen Fernandez-Metzler
Joseph J. Salata
George D. Hartman
Source :
Bioorganicmedicinal chemistry letters. 17(19)
Publication Year :
2007

Abstract

3,5-diaryl-4,5-dihydropyrazoles were discovered to be potent KSP inhibitors with excellent in vivo potency. These enzyme inhibitors possess desirable physical properties that can be readily modified by incorporation of a weakly basic amine. Careful adjustment of amine basicity was essential for preserving cellular potency in a multidrug resistant cell line while maintaining good aqueous solubility.

Details

ISSN :
0960894X
Volume :
17
Issue :
19
Database :
OpenAIRE
Journal :
Bioorganicmedicinal chemistry letters
Accession number :
edsair.doi.dedup.....5b61cc6362d9b2c03266cc85d1b2a289